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Autologous Engineered Skin Substitutes for Closure of Skin Wounds

2014-07-24 14:19:18 | BioPortfolio

Summary

This clinical trial tests the hypothesis that engineered human skin can reduce the requirements for harvesting of conventional skin autografts by providing more skin for grafting from the donor skin used to treat the wounds. In life-threatening burns (e.g., greater than 50% of the total body surface area), greater availability of skin may be definitive to patient survival, and may reduce scar formation at the donor site, and from use of widely-meshed skin autograft.

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Conditions

Burns, Burn Scars, Congenital Giant Nevi

Intervention

Autologous engineered skin substitutes, Autologous Engineered Skin Substitutes

Status

Suspended

Source

University of Cincinnati

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-07-24T14:19:18-0400

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